KEGG   Prionailurus viverrinus (fishing cat): 125171980
Entry
125171980         CDS       T09889                                 
Symbol
WNT2B
Name
(RefSeq) protein Wnt-2b isoform X1
  KO
K00182  wingless-type MMTV integration site family, member 2
Organism
pviv  Prionailurus viverrinus (fishing cat)
Pathway
pviv04150  mTOR signaling pathway
pviv04310  Wnt signaling pathway
pviv04390  Hippo signaling pathway
pviv04550  Signaling pathways regulating pluripotency of stem cells
pviv04916  Melanogenesis
pviv04934  Cushing syndrome
pviv05010  Alzheimer disease
pviv05022  Pathways of neurodegeneration - multiple diseases
pviv05165  Human papillomavirus infection
pviv05200  Pathways in cancer
pviv05205  Proteoglycans in cancer
pviv05217  Basal cell carcinoma
pviv05224  Breast cancer
pviv05225  Hepatocellular carcinoma
pviv05226  Gastric cancer
Brite
KEGG Orthology (KO) [BR:pviv00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04310 Wnt signaling pathway
    125171980 (WNT2B)
   04390 Hippo signaling pathway
    125171980 (WNT2B)
   04150 mTOR signaling pathway
    125171980 (WNT2B)
 09140 Cellular Processes
  09144 Cellular community - eukaryotes
   04550 Signaling pathways regulating pluripotency of stem cells
    125171980 (WNT2B)
 09150 Organismal Systems
  09152 Endocrine system
   04916 Melanogenesis
    125171980 (WNT2B)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    125171980 (WNT2B)
   05205 Proteoglycans in cancer
    125171980 (WNT2B)
  09162 Cancer: specific types
   05225 Hepatocellular carcinoma
    125171980 (WNT2B)
   05226 Gastric cancer
    125171980 (WNT2B)
   05217 Basal cell carcinoma
    125171980 (WNT2B)
   05224 Breast cancer
    125171980 (WNT2B)
  09172 Infectious disease: viral
   05165 Human papillomavirus infection
    125171980 (WNT2B)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    125171980 (WNT2B)
   05022 Pathways of neurodegeneration - multiple diseases
    125171980 (WNT2B)
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    125171980 (WNT2B)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   00536 Glycosaminoglycan binding proteins [BR:pviv00536]
    125171980 (WNT2B)
Glycosaminoglycan binding proteins [BR:pviv00536]
 Heparan sulfate / Heparin
  Morphogens
   125171980 (WNT2B)
SSDB
Motif
Pfam: wnt DUF6973
Other DBs
NCBI-GeneID: 125171980
NCBI-ProteinID: XP_047725289
LinkDB
Position
C1:complement(118124991..118141306)
AA seq 393 aa
MLKPGGAEEAAQLLPRRARAPVPALPPGPAAPDGSRASARLGLACLLLLLLLTLPARVDT
SWWYIGALGARVICDNIPGLVSRQRQLCQRYPDIMRSVGEGAREWIRECQHQFRHHRWNC
TTLDRDHTVFGRVMLRSSREAAFVYAISSAGVVHAITRACSQGELSVCSCDPYTRGRHHD
QRGDFDWGGCSDNIHYGVRFAKAFVDAKEKRLKDARALMNLHNNRCGRTAVRRFLKLECK
CHGVSGSCTLRTCWRALSDFRRTGDYLRRRYDGAVQVTATQDGANFTAARQGYRRATRTD
LVYFDNSPDYCVLDKAAGSLGTAGRVCSKTSKGTDGCEIMCCGRGYDTTRVTRVTQCECK
FHWCCAVRCKECRNTVDVHTCKAPKKAEWLDQT
NT seq 1182 nt   +upstreamnt  +downstreamnt
atgctgaagccgggtggtgcggaggaagccgcacagctcctccctcggcgcgcccgcgcc
cctgtccccgcgctcccgccaggacccgcggcccccgacggctctcgggcttcggcccgc
ctcggtcttgcctgcctgctgttgctgctgctgctgacgctgccggcccgcgtagacacg
tcctggtggtacatcggggcactgggggcccgagtgatctgtgacaatatccctggtctg
gtgagccggcagcggcagttgtgccagcgttacccagacatcatgcgctcggtgggcgag
ggtgcccgagaatggatccgagagtgtcagcaccagttccgccaccaccgctggaactgc
accacgctggaccgggaccacactgtctttggccgtgtcatgctcagaagcagccgggag
gcagcatttgtatatgccatctcgtctgcaggggtggtccatgctatcactcgtgcctgc
agccagggagaactgagtgtgtgcagctgtgacccctacacccgtggccgacaccatgac
caacgtggggattttgactggggtggctgcagtgacaacatccattatggtgttcgcttt
gccaaggcctttgtggatgccaaggaaaagaggcttaaggatgcccgggccctcatgaac
ttacataacaaccgctgtggtcgcacggctgtgcggcggtttctgaagctcgagtgtaag
tgccatggcgttagtggctcctgtactctgcgcacctgctggcgtgcactctcagacttc
cgccgcacaggtgattacctgcggcggcgctacgatggggctgtgcaggtgacagcaacc
caggatggcgccaacttcacagcagcccgccaaggttatcgccgtgccacccggactgac
cttgtctactttgacaactccccagactactgtgtcttagacaaggctgcaggttcccta
ggcactgcgggccgtgtctgtagcaagacatccaaagggacggatggttgcgaaatcatg
tgctgtggccgagggtacgacacaactcgagtcacccgtgtcacccagtgtgagtgcaaa
ttccactggtgctgtgcagtgcggtgcaaggagtgcagaaacactgtggacgtccacact
tgcaaggcccccaagaaggcagagtggctggaccagacctga

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